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The proteomic profile of hereditary inclusion body myopathy.
Sela I, Milman Krentsis I, Shlomai Z, Sadeh M, Dabby R, Argov Z, Ben-Bassat H, Mitrani-Rosenbaum S. Sela I, et al. Among authors: sadeh m. PLoS One. 2011 Jan 31;6(1):e16334. doi: 10.1371/journal.pone.0016334. PLoS One. 2011. PMID: 21305017 Free PMC article.
Survival-apoptosis associated signaling in GNE myopathy-cultured myoblasts.
Harazi A, Chaouat M, Shlomai Z, Levitzki R, Becker-Cohen M, Sadeh M, Dabby R, Ben-Bassat H, Mitrani-Rosenbaum S. Harazi A, et al. Among authors: sadeh m. J Recept Signal Transduct Res. 2015;35(4):249-57. doi: 10.3109/10799893.2014.956755. Epub 2014 Dec 16. J Recept Signal Transduct Res. 2015. PMID: 25510413
Mitochondrial processes are impaired in hereditary inclusion body myopathy.
Eisenberg I, Novershtern N, Itzhaki Z, Becker-Cohen M, Sadeh M, Willems PH, Friedman N, Koopman WJ, Mitrani-Rosenbaum S. Eisenberg I, et al. Among authors: sadeh m. Hum Mol Genet. 2008 Dec 1;17(23):3663-74. doi: 10.1093/hmg/ddn261. Epub 2008 Aug 23. Hum Mol Genet. 2008. PMID: 18723858
The homozygous M712T mutation of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase results in reduced enzyme activities but not in altered overall cellular sialylation in hereditary inclusion body myopathy.
Hinderlich S, Salama I, Eisenberg I, Potikha T, Mantey LR, Yarema KJ, Horstkorte R, Argov Z, Sadeh M, Reutter W, Mitrani-Rosenbaum S. Hinderlich S, et al. Among authors: sadeh m. FEBS Lett. 2004 May 21;566(1-3):105-9. doi: 10.1016/j.febslet.2004.04.013. FEBS Lett. 2004. PMID: 15147877 Free article.
Facial weakness in hereditary inclusion body myopathies.
Argov Z, Sadeh M, Eisenberg I, Karpati G, Mitrani-Rosenbaum S. Argov Z, et al. Among authors: sadeh m. Neurology. 1998 Jun;50(6):1925-6. doi: 10.1212/wnl.50.6.1925. Neurology. 1998. PMID: 9633772 No abstract available.
248 results